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Recombinant human granulocyte colony-stimulating factor increases circulating CD34-postive cells in patients with
S D Nielsen1, S Dam-Larsen, C Nielsen
1Department of Infectious Diseases, Hvidovre Hospital, Denmark.
Annals of Hematology
|May 1, 1997
Summary
Recombinant human granulocyte colony-stimulating factor (G-CSF) effectively increases circulating hematopoietic progenitor cells (CD34 cells) in AIDS patients without enhancing HIV replication, supporting its use in gene therapy. This study offers a potential strategy for improving gene therapy efficacy.
Area of Science:
- Hematology
- Gene Therapy
- Virology
Background:
- Gene therapy for AIDS requires a high number of target cells.
- The number of circulating hematopoietic progenitor cells (CD34 cells) is a limiting factor in AIDS gene therapy.
- Neutropenia is common in AIDS patients.
Purpose of the Study:
- To investigate if recombinant human granulocyte colony-stimulating factor (G-CSF) can increase the absolute number of CD34 cells in AIDS patients.
- To assess the safety of G-CSF treatment in AIDS patients, specifically regarding HIV replication.
Main Methods:
- Eight patients with AIDS and neutropenia were treated with daily subcutaneous injections of 300 micrograms G-CSF for 3-5 days.
- Absolute neutrophil count (ANC) and absolute CD34 cell counts were monitored.
- HIV-1 RNA PCR was used to detect changes in HIV replication.
Main Results:
- G-CSF treatment led to a significant increase in ANC in all patients, from a median of 0.4 to 3.4 x 10(9)/l.
- G-CSF significantly increased the absolute number of CD34 cells, with a median rise from 0.8 to 2.2 x 10(6)/l.
- HIV-1 RNA PCR showed no enhanced HIV replication in patients treated with G-CSF.
Conclusions:
- G-CSF can be safely used to mobilize CD34 cells in patients with AIDS.
- The mobilization of CD34 cells by G-CSF may enhance the feasibility of gene therapy protocols for AIDS.
- G-CSF treatment offers a potential strategy to increase target cells for AIDS gene therapy without exacerbating viral load.